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Clinical Trial Summary

The purpose of this clinical study is to obtain human clinical data that demonstrates that the size 23mm Carpentier-Edwards PERIMOUNT Magna mitral pericardial valve, model 7000TFX, is a safe and effective replacement heart valve.


Clinical Trial Description

This is a prospective, non-randomized, multi-site, descriptive study. A minimum of 15 and up to 20 subjects will be implanted at a minimum of 2 and up to 8 participating investigational sites within the US and internationally. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01312779
Study type Interventional
Source Edwards Lifesciences
Contact
Status Completed
Phase N/A
Start date March 2011
Completion date November 2018